Fröjdman K, Ekblom P, Sorokin L, Yagi A, Pelliniemi L J
Laboratory of Electron Microscopy, University of Turku, Finland.
Int J Dev Biol. 1995 Apr;39(2):335-44.
The distribution of laminin chains and basement membranes (BMs) in the ontogenesis and sex differentiation of male and female mouse gonads and mesonephros was studied by conventional and immunocytochemical light and electron microscopy. The alpha 1 (synonymous to A) chain was recognized with MAbs against fragment E3, and three chains of laminin with PAbs raised against EHS-laminin. BMs, which formed around the mesonephric duct, the mesonephric tubules, and the paramesonephric duct, contained the laminin alpha 1 chain. The alpha 1 chain appeared with epithelial differentiation in the developing gonads in both sexes. The alpha 1 chain was first evident around the embryonic gonadal cords and remained, after development, in the BMs of the testicular cords and ovarian follicles. The laminin alpha 1 chain was also detected in BMs of the myoid cells around the epithelial rete cords, and transiently in the surface epithelium and in the corpus luteum. Laminin beta-gamma chains were found in many locations where the alpha 1 chain was not detected. These included the mesenchyme of the early mesonephros, the BMs of blood vessels and surface epithelium in the differentiated testis and ovary, between the theca cells in the ovary, and in some corpora lutea. The morphological differentiation of the BMs of the embryonic testicular cords proceeded rapidly. In contrast, the BM of the ovarian cords remained relatively poorly differentiated during the prenatal phases, and developed concomitantly with the differentiation of the follicles. The results show that BMs in the differentiating internal genitalia are heterogeneous with respect to their laminin chains, and suggest that all known laminin chains must be analyzed in the differentiation of gonadal epithelia for a complete role of the BMs in gonadal sex differentiation.
通过传统及免疫细胞化学光镜和电镜技术,研究了层粘连蛋白链和基底膜(BMs)在雄性和雌性小鼠性腺及中肾发生和性别分化过程中的分布。用抗片段E3的单克隆抗体识别α1(等同于A)链,用抗EHS-层粘连蛋白产生的多克隆抗体识别层粘连蛋白的三条链。围绕中肾管、中肾小管和副中肾管形成的BMs含有层粘连蛋白α1链。α1链在两性发育中的性腺上皮分化时出现。α1链最初在胚胎性腺索周围明显可见,发育后保留在睾丸索和卵巢卵泡的BMs中。层粘连蛋白α1链也在上皮网索周围的肌样细胞的BMs中检测到,并短暂出现在表面上皮和黄体中。在许多未检测到α1链的位置发现了层粘连蛋白β-γ链。这些位置包括早期中肾的间充质、分化的睾丸和卵巢中的血管和表面上皮的BMs、卵巢卵泡膜细胞之间以及一些黄体中。胚胎睾丸索的BMs的形态分化进展迅速。相比之下,卵巢索的BM在产前阶段分化相对较差,并随着卵泡的分化而发育。结果表明,分化中的内生殖器的BMs在层粘连蛋白链方面是异质性的,这表明在性腺上皮分化过程中,必须分析所有已知的层粘连蛋白链,以便全面了解BMs在性腺性别分化中的作用。